(Q57628942)

English

Absence of previously reported variants in theSCNA (G88C and G209A),NR4A2 (T291D and T245G) and theDJ-1 (T497C) genes in familial Parkinson's disease from theGenePD study

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15966003%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study (English)

1 reference

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13 January 2020

Parkinson's disease

1 reference

based on heuristic

inferred from title

Marie-Helene Saint-Hilaire

11

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13 January 2020

Jeanne C Latourelle

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13 January 2020

Richard H Myers

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13 January 2020

Joel S Perlmutter

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object named as

J S Perlmutter

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13 January 2020

author name string

Samer Karamohamed

1

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13 January 2020

Mark Guttman

7

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13 January 2020

Carlos Singer

29

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13 January 2020

L I Golbe

2

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13 January 2020

M H Mark

3

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13 January 2020

A M Lazzarini

4

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13 January 2020

O Suchowersky

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13 January 2020

N Labelle

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13 January 2020

L J Currie

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13 January 2020

G F Wooten

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13 January 2020

M Stacy

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13 January 2020

R G Feldman

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13 January 2020

J Liu

13

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13 January 2020

C M Shoemaker

14

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13 January 2020

J B Wilk

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13 January 2020

A L DeStefano

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13 January 2020

G Xu

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13 January 2020

R Watts

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13 January 2020

J Growdon

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13 January 2020

M Lew

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13 January 2020

C Waters

22

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13 January 2020

P Vieregge

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13 January 2020

P P Pramstaller

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13 January 2020

C Klein

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13 January 2020

B A Racette

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13 January 2020

A Parsian

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13 January 2020

E Montgomery

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13 January 2020

K Baker

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13 January 2020

J F Gusella

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13 January 2020

A Herbert

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13 January 2020

language of work or name

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publication date

1 September 2005

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13 January 2020

Movement Disorders

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13 January 2020

20

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13 January 2020

1188-1191

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13 January 2020

9

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13 January 2020

Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20515

21 January 2018

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20515

21 January 2018

Identifiers

10.1002/MDS.20515

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13 January 2020

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13 January 2020

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